481-46-9 Usage
Description
GINKGETIN is a biflavonoid that is the 7,4'-dimethyl ether derivative of amentoflavone. It is isolated from Ginkgo biloba and Dioon, and it exhibits various biological activities, including anti-HSV-1, antineoplastic, and inhibitory effects on arachidonate 5-lipoxygenase and cyclooxygenase 2.
Uses
Used in Pharmaceutical Industry:
GINKGETIN is used as an antiviral agent for its anti-HSV-1 activity, helping to combat herpes simplex virus type 1 infections.
Used in Anticancer Applications:
GINKGETIN is used as an antineoplastic agent, contributing to the inhibition of cancer cell growth and proliferation.
Used in Inflammation Management:
GINKGETIN is used as an inhibitor for arachidonate 5-lipoxygenase and cyclooxygenase 2, playing a role in reducing inflammation and pain.
Used in Nutraceutical Industry:
GINKGETIN can be used as a dietary supplement due to its various health-promoting properties, such as its antiviral, anticancer, and anti-inflammatory effects.
Used in Cosmetic Industry:
GINKGETIN may be used in the development of skincare products, leveraging its anti-inflammatory and potential anti-aging properties to improve skin health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 481-46-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 481-46:
(5*4)+(4*8)+(3*1)+(2*4)+(1*6)=69
69 % 10 = 9
So 481-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H22O10/c1-39-18-10-20(34)30-23(37)13-27(41-28(30)11-18)16-5-8-25(40-2)19(9-16)29-21(35)12-22(36)31-24(38)14-26(42-32(29)31)15-3-6-17(33)7-4-15/h3-14,33-36H,1-2H3
481-46-9Relevant articles and documents
A new strategy for the synthesis of biflavonoids via arylboronic acids
Muller, Dominique,Fleury, Jean-Pierre
, p. 2229 - 2232 (2007/10/02)
Amentoflavone derivatives were prepared by catalytic coupling of 8-flavone-boronic acids with iodoflavones. 3-Arylflavones, as biflavonoid synthon, are accessible by the method.